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A standard operating procedure or simply SOP is a particular operation that needs to be done in accordance with the rules and guidelines of a company or an industry. It is an important way for a company to run smoothly, especially in small businesses. It is like a practice wherein everything an individual or an employee is under a particular standard that is implemented.

GMP stands for Good Manufacturing Practice. It is a system that ensures that all products like food, beverages, and medicinal drugs that are produced comply with the quality standards. It helps in minimizing the risks and hazards that cannot be eliminated after the testing of final products.

Technical reports are a type of document that is used to indicate either the progress, result, or process of scientific research or the state of problems occurring within such research. A technical report may also showcase the report's overall conclusion and may also include recommendations. This kind of report does not require a peer review and isn't published officially but distributed within the organizations where it was formed.

Quality control is a set of instructions or procedures to ensure a manufactured product or a service is up to the highest quality standards. This set of quality control criteria are either defined by the clients or the company itself.

Assay development is a process in molecular biology to test or measure the activity of a drug or biochemical substance in an organic sample or organism and to screen putative compounds to determine the interaction and/or modification of the target. The aim is to standardize the assay and to be able to use it repeatedly and reproducibly.

CMC stands for "chemistry, manufacturing, and controls," which represents a standard procedure when producing new pharmaceutical drugs. First the drug is developed through chemical tests and analysis, then the drug is manufactured. Before the pharmaceutical can be offered to the public, it must be tested on individuals, often animal test subjects first and then human beings. This allows pharmacists to determine whether the drug must be reconsidered, reproduced, or whether any side effects accompany the drug.

The Food and Drug Administration (FDA) is a division of the US Department of Health and Human Services that regulates the production and sale of food, pharmaceutical products, medical equipment, and other consumer goods, as well as veterinary medicine. The FDA is now in charge of overseeing the manufacture of products like vaccines, allergy treatments, and beauty products.

DOE, DOX, or design of experiments is a term used to refer to a part of applied statistics whose main focus is to conduct and observe controlled tests with the ultimate goal of understanding and explaining how information and results might vary under different hypotheses and circumstances and how such variables affect the results and tests. Design of experiments is used in marketing, politics, various sciences, and, of course, experiments.

A LIMS - Laboratory Information Management System is a software solution to improve laboratory productivity and efficiency with modern support of laboratory operations to address the challenges of data and sample management, automation, and regulation of laboratories from around the world and thus maintaining workflows and standardized testing and reporting procedures.

A drug product is a drug that has the finished dosage form which is the final product from a pharmaceutical company bearing an active ingredient. The active ingredient is tagged along with other inactive ingredients that make the product whole in the effect that it offer to users.